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一种基于β-己糖胺酶的拟过敏评估新方法及其在中药注射液中的应用。

A novel method for evaluating pseudoallergy based on β-hexosaminidase and its application for traditional Chinese medicine injections.

机构信息

Jiangsu Key Laboratory of TCM Evaluation and Translational Research, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, P. R. China.

出版信息

J Sep Sci. 2024 Jan;47(1):e2300545. doi: 10.1002/jssc.202300545.

Abstract

Pseudoallergy is a typical and common adverse drug reaction to injections, especially in traditional Chinese medicine injections (TCMIs). At present, the evaluation methods for pseudoallergy include cell methods in vitro and animal methods in vivo. The mast cell evaluation method based on the β-hexosaminidase (β-Hex)-catalyzed substrate, 4-nitrophenyl-β-N-acetyl-D-glucosaminide (4-NPG), is an important method for the evaluation of drug-induced pseudoallergy, but it is prone to false positive results and has insufficient sensitivity. In this study, a novel β-Hex evaluation system with rat basophilic leukemia-2H3 cells based on high-performance liquid chromatography-fluorescence detection (HPLC-FLD) was established, which effectively increased the sensitivity and avoided false positive results. Cell viabilities were measured by 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl tetrazolium bromide assay. In addition, a method for the determination of histamine, which is another indicator in the development of pseudoallergy, was established to validate the above method. The results of this novel method indicated that two TCMIs (Shuxuening injection and Shenqi Fuzheng injection), which were considered to be pseudoallergenic using 4-NPG, were not pseudoallergenic. Overall, the novel β-Hex/HPLC-FLD evaluation system using Rat basophilic leukemia-2H3 cells established was effective and precise. It could be used for the evaluation of pseudoallergic reactions caused by TCMIs and other injections.

摘要

假性过敏是注射剂特别是中药注射剂(TCMIs)中一种典型且常见的药物不良反应。目前,假性过敏的评价方法包括体外细胞方法和体内动物方法。基于β-己糖胺酶(β-Hex)催化底物 4-硝基苯-β-N-乙酰-D-氨基葡萄糖苷(4-NPG)的肥大细胞评价方法是评价药物诱导假性过敏的重要方法,但易出现假阳性结果且灵敏度不足。本研究建立了一种基于高效液相色谱-荧光检测(HPLC-FLD)的新型大鼠嗜碱性白血病-2H3 细胞 β-Hex 评价系统,该系统有效提高了灵敏度,避免了假阳性结果。通过 3-(4,5-二甲基-2-噻唑基)-2,5-二苯基四氮唑溴盐法(3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl tetrazolium bromide assay)测定细胞活力。此外,还建立了一种测定另一种假性过敏发展指标组胺的方法,以验证上述方法。该新型方法的结果表明,两种被认为是假性过敏的 TCMIs(舒血宁注射液和参芪扶正注射液)实际上并不具有假性过敏。总体而言,使用大鼠嗜碱性白血病-2H3 细胞建立的新型β-Hex/HPLC-FLD 评价系统有效且精确。它可用于评价 TCMIs 和其他注射剂引起的假性过敏反应。

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